Canonical Allele Identifier: CA515262178
Gene: SHANK3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.51159799G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50721371G>T , CM000684.2:g.50721371G>T GRCh38
NC_000022.10:g.51159799G>T , CM000684.1:g.51159799G>T GRCh37
NC_000022.9:g.49506665G>T NCBI36
NG_008607.2:g.52017G>T
NG_070230.1:g.57155G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262795.7:c.3139G>T ENSP00000489147.2:p.Val1047Phe
ENST00000414786.7:n.3723G>T
ENST00000445220.7:c.2191G>T ENSP00000489407.2:p.Val731Phe
ENST00000664402.2:c.1681G>T ENSP00000499475.1:p.Val561Phe
ENST00000673971.2:c.*2137G>T ENSP00000501192.1:n.*2137G>T
ENST00000445220.6:c.2191G>T ENSP00000489407.2:p.Val731Phe
ENST00000262795.6:c.3139G>T ENSP00000489147.2:p.Val1047Phe
ENST00000664402.1:c.1681G>T ENSP00000499475.1:p.Val561Phe
ENST00000673971.1:c.*2137G>T ENSP00000501192.1:n.*2137G>T
ENST00000262795.5:c.3535G>T ENSP00000489147.1:p.Val1179Phe
ENST00000414786.6:n.3723G>T
ENST00000445220.5:c.3517G>T ENSP00000489407.1:p.Val1173Phe